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3-p-Tolylselanyl-propionic acid, also known as 3-(4-methylphenyl)selanyl-propionic acid, is an organoselenium compound characterized by the presence of a selenoether group (a selenium analog of an ether) and a propionic acid functional group. 3-p-Tolylselanyl-propionic acid features a 4-methylphenyl (p-tolyl) group attached to a selenium atom, which is in turn connected to a propionic acid chain. The structure of 3-p-tolylselanyl-propionic acid can be represented as C6H4CH3-CH2-Se-CH2CH2COOH. It is an odorless, white crystalline solid that is soluble in organic solvents. 3-p-Tolylselanyl-propionic acid has potential applications in the field of organic synthesis and may be of interest in the development of new materials or pharmaceuticals due to its unique structure and properties.

6534-91-4

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6534-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6534-91-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6534-91:
(6*6)+(5*5)+(4*3)+(3*4)+(2*9)+(1*1)=104
104 % 10 = 4
So 6534-91-4 is a valid CAS Registry Number.

6534-91-4Downstream Products

6534-91-4Relevant academic research and scientific papers

Design, synthesis and biological evaluation of novel semicarbazone-selenochroman-4-ones hybrids as potent antifungal agents

Xu, Hang,Su, Xin,Liu, Xiao-qian,Zhang, Kai-peng,Hou, Zhuang,Guo, Chun

supporting information, (2019/10/19)

A series of novel 2,3-dihydro-4H-1-benzoselenin-4-one (thio)semicarbazone derivatives were designed and synthesized by using molecular hybridization approach. All the target compounds were characterized by HRMS and NMR and evaluated in vitro antifungal activity against five pathogenic strains. In comparison with precursor selenochroman-4-ones, the hybrid molecules in this study showed significant improvement in antifungal activities. Notably, compound B8 showed significant antifungal activity against other strains excluding Aspergillus fumigatus (0.25 μg/mL on Candida albicans, 2 μg/mL on Cryptococcus neoformans, 8 μg/mL on Candida zeylanoides and 2 μg/mL on fluconazole-sensitive strains of Candida albicans). Moreover, compounds B8, B9 and C2 also displayed most potent activities against four fluconazole-resistance strains. Especially the MIC values of the hybrid molecule B8 against fluconazole-resistant strains were in the range of 0.5–2 μg/mL. Therefore, the molecular hybridization approach in this study provided new ideas for the development of antifungal drug.

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